E. Friauf et al., DEVELOPMENT OF ADULT-TYPE INHIBITORY GLYCINE RECEPTORS IN THE CENTRALAUDITORY-SYSTEM OF RATS, Journal of comparative neurology, 385(1), 1997, pp. 117-134
Inhibitory synaptic activity is crucial for many aspects of acoustic i
nformation processing and mainly mediated by glycine and gamma-aminobu
tyric acid, the two principal inhibitory neurotransmitters in the audi
tory system. Glycine exerts its inhibitory action via binding to posts
ynaptic receptors existing in various isoforms. Here we have investiga
ted the spatiotemporal distribution of adult-type, strychnine-sensitiv
e glycine receptors (GlyRs) in the rat auditory system by using a spec
ific antibody against the ligand-binding alpha 1 GlyR subunit. In adul
ts, alpha 1 GlyRs were found at all relay stations of the auditory pat
hway except for the medial geniculate body and the auditory cortex. In
most brainstem nuclei, labeling was characterized by dense clusters o
f heavily immunoreactive puncta outlining the somata and proximal dend
rites, indicative of a powerful glycinergic inhibition. No alpha 1 imm
unoreactivity was seen in the auditory system of fetal rats, consisten
t with results obtained by others in the spinal cord. At birth, labeli
ng was weak and restricted to defined nuclei of the cochlear nuclear c
omplex and the superior olivary complex. By postnatal day 8, labeling
was seen in all brainstem nuclei. At the first appearance of immunorea
ctivity, alpha 1 GlyRs were diffusely distributed on the neuronal surf
ace, yet they became clustered with age, finally densely incrusting th
e somata and proximal dendrites between the 3rd and 4th postnatal week
, when the mature pattern of immunoreactivity was established. We neve
r observed an overexpression of alpha 1 GlyRs or a transient appearanc
e in areas that are devoid of the receptor in adults. The late formati
on of glycinergic synapses harboring the adult-type GlyRs in the audit
ory system, at a time when internuclear connections have already forme
d, indicates that alpha 1 GlyRs do not participate in early synaptogen
esis. (C) 1997 Wiley-Liss, Inc.